“…Often, responses to differences in seagrass meadows are observed only for certain taxa within the community, only at certain scales, or only in certain time periods (Heck and Thoman, 1984;Bell and Westoby, 1986a,b;Hovel et al, 2002;Jelbart et al, 2007;Moore and Hovel, 2010;McCloskey and Unsworth, 2015). In addition, factors other than seagrass complexity can influence seagrassassociated faunal communities, such as nutrient enrichment (Hooks et al, 1976;Gil et al, 2006;Peterson et al, 2007;Armitage and Fourqurean, 2009;Daudi et al, 2012;Burghart et al, 2013;Tuya et al, 2013), exposure to waves and tides as determined by position within the estuary (Bell and Westoby, 1986b;Jelbart et al, 2007;Moore and Hovel, 2010;Parsons et al, 2013;Ávila et al, 2015), storms or other large-scale physical disturbances (Herkül et al, 2011;Patrick et al, 2020), and predation pressure (Stoner, 1980;Heck et al, 2000;Heck and Valentine, 2007;Mattila et al, 2008;Amundrud et al, 2015;Huang et al, 2015). Therefore, despite decades of effort, relatively few generalizable relationships have emerged that link differences in seagrass-associated faunal communities with metrics of seagrass complexity, particularly at spatial scales of kilometers or more (Boström et al, 2006), perhaps due to the challenges of finding suitable variation in environmental conditions and the complexity of meadows comprising one species of seagrass at such scales (e.g., Cardoso et al, 2007).…”